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1 . 2,4,4'-trimethoxyflavone-2'-hydroxychalcone C18H18O5 ÏàËÆ¶È:61.1% Journal of Chemical Research 2006 30 163-164 First total synthesis of two 5-deoxyflavone derivatives from Albizia odoratissima Gao, Jin-Ming; Lu, Jia-Wen; Zhang, An-Ling; Cheng, Yong-Xian; Watchueng, Jean; Konishi, Yasuo Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 2 . (E)-1-[4-(allyloxy)-2-hydroxyphenyl]-3-(2,4-dimethoxyphenyl)prop-2-en-1-one C20H20O5 ÏàËÆ¶È:60% Bioorganic & Medicinal Chemistry 2011 19 7711-7719 Structure¨Cactivity relationships of chalcone analogs as potential inhibitors of ADP- and collagen-induced platelet aggregation M. Vijaya Bhaskar Reddy, Wei-Jern Tsai, Keduo Qian, Kuo-Hsiung Lee, Tian-Shung Wu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 3 . (E)-1-(2-Hydroxy-4-methoxyphenyl)-3-(3-methoxyphenyl)prop-2-en-1-one C17H16O4 ÏàËÆ¶È:58.8% Bioorganic & Medicinal Chemistry 2012 20 346-355 Investigation of chalcones and benzochalcones as inhibitors of breast cancer resistance protein Kapil Juvale, Veronika F.S. Pape, Michael Wiese Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 4 . 4-Hydroxy-2-(4'-hydroxy-2'-methoxyphenyl)-6-methoxybenzofuran¨C3-carbaldehyde C17H13O6 ÏàËÆ¶È:58.8% Journal of Natural Medicines 2009 63 189-191 A new arylbenzofuran from the aerial parts of alfalfa Shengchao Wang, Guogang Zhang, Jin Guan, Linxia Zhu and Lijuan Chen, et al. Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 5 . cajanol C17H16O6 ÏàËÆ¶È:58.8% Journal of Shenyang Pharmaceutical University 2008 25 448-453 Flavonoids from Campylotropis hirtella (Franch.) Schindl. and their bioactivities WEN Ping, HAN Hui-ying, WANG Nai-li, YAO Xin-sheng Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 6 . 4,4'-Dihydroxy-2'-methoxy-chalcone ÏàËÆ¶È:58.8% Journal of the Brazilian Chemical Society 2005 16 1402-1405 Biflavonoids and other Phenolics from Caesalpinia pyramidalis (Fabaceae) Marcus V. Bahia, Jamile B. dos Santos, Juceni P. David and Jorge M. David Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 7 . uncinanone E C18H18O6 ÏàËÆ¶È:55.5% Phytochemistry 2007 68 646-651 C-methylated and C-prenylated isoflavonoids from root extract of Desmodium uncinatum Salome M. Guchu, Abiy Yenesew, Muniru K. Tsanuo, Nicholas K. Gikonyo,John A. Pickett, Antony M. Hooper, Ahmed Hassanali Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 8 . Gandavensin G C18H14O7 ÏàËÆ¶È:55.5% Journal of Asian Natural Products Research 2005 7 197-204 Anthraquinones from Gladiolus gandavensis BIN CHEN, DING-YONG WANG, QI YE, BO-GANG LI and GUO-LIN ZHANG Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 9 . (E)-3-(2,4-dimethoxyphenyl)-1-[2-hydroxy-4-(3-methylbut-2-enyloxy)phenyl]prop-2-en-1-one C22H24O5 ÏàËÆ¶È:54.5% Bioorganic & Medicinal Chemistry 2011 19 7711-7719 Structure¨Cactivity relationships of chalcone analogs as potential inhibitors of ADP- and collagen-induced platelet aggregation M. Vijaya Bhaskar Reddy, Wei-Jern Tsai, Keduo Qian, Kuo-Hsiung Lee, Tian-Shung Wu Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 10 . spinosan B C17H14O5 ÏàËÆ¶È:52.9% Journal of Natural Products 2006 69 261-264 Metabolites of the ¡°Smoke Tree¡±, Dalea spinosa, Potentiate Antibiotic Activity against Multidrug-Resistant Staphylococcus aureus Gil Belofsky, Roberto Carreno, Kim Lewis, Anthony Ball, Gabriele Casadei, and George P. Tegos Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 11 . compound 4 C20H20O8 ÏàËÆ¶È:52.9% Journal of Natural Products 2002 65 48-50 Cryphonectric Acid and Other Minor Metabolites from a Hypovirulent Strain of Cryphonectria parasitica1 Alberto Arnone,Gemma Assante, Gianluca Nasini, Sara Strada, and Annamaria Vercesi Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 12 . compound 10 ÏàËÆ¶È:52.9% Chemical & Pharmaceutical Bulletin 1980 28 708-716 13C-Nuclear Magnetic Resonance (NMR) Spectral Studies on Polysubstituted Flavonoids. I. 13C-NMR Spectra of Flavones MUNEKAZU IINUMA,SHIN MATSUURA and KOUSUKE KUSUDA Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 13 . 4,2'-dihydroxy-4'-methoxy chalcone ÏàËÆ¶È:52.9% China Journal of Chinese Materia Medica 2008 33 1292-1294 Studies on Chemical Constituents of Oxytropis falcata WANG Dong, YANG Huan, DAI Yan-peng, TONG Li, CAI Bao-chang Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 14 . 1-(2-hydroxy-4-methoxyphenyl)-3-(3,4-methylenedioxyphenyl) propan-2-ol ÏàËÆ¶È:52.9% Phytochemistry 2000 53 155-157 An isoflavone from Myristica malabarica A.C. Talukdar, Niveta Jain, Shantanu De, H.G. Krishnamurty Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 15 . 2'-hydroxy-5'-methoxybiochanin A C17H14O7 ÏàËÆ¶È:52.9% Journal of Natural Products 1989 Vol 52 320 Two New Flavonoids from Erythrina eriotriocha Augustin E. Nkengfack, Dale R. Sanson, Michael S. Tempesta, Z. Tanee Fomum Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 16 . luteolin-5,3'-dimethyl ether C17H14O6 ÏàËÆ¶È:52.9% Acta Pharmaceutica Sinica 2007 Vol 42 174-178 Isolation and identification of phenolic constituents from Juncus effusus LI Hong-xia; DENG Tie-zhong; CHEN Yu; FENG Hui-jin; YANG Guang-zhong Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 17 . compound 1d ÏàËÆ¶È:52.9% Phytochemistry 1995 40 271-274 Chalcone and dihydrochalcone derivatives from the orchid Lusia volucris P. L. Majumder, S. Lahiri, N. Mukhoti Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 18 . (E)-1-(2-Hydroxy-4-methoxyphenyl)-3-(4-methoxyphenyl)prop-2-en-1-one C17H16O4*0.2H2O ÏàËÆ¶È:52.9% Bioorganic & Medicinal Chemistry 2012 20 346-355 Investigation of chalcones and benzochalcones as inhibitors of breast cancer resistance protein Kapil Juvale, Veronika F.S. Pape, Michael Wiese Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 19 . (E)-3-(2-Chlorophenyl)-1-(2-hydroxy-4,6-dimethoxyphenyl)prop-2-en-1-one C17H15ClO4 ÏàËÆ¶È:52.9% Bioorganic & Medicinal Chemistry 2012 20 346-355 Investigation of chalcones and benzochalcones as inhibitors of breast cancer resistance protein Kapil Juvale, Veronika F.S. Pape, Michael Wiese Structure 13C NMR ̼Æ×Ä£Äâͼ -------------------------------------------------------------------------------- 20 . 2',4'-Dihydroxy-2,4-dimethoxychalcone C17H16O5 ÏàËÆ¶È:52.9% Bioorganic & Medicinal Chemistry 2012 20 25-33 Solid-phase synthesis of 20-hydroxychalcones. Effects on cell growth inhibition, cell cycle and apoptosis of human tumor cell lines Marta Perro Neves, Sara Cravo, Raquel T. Lima,M. Helena Vasconcelos,M. São Jos¨¦ Nascimento, Artur M.S. Silva, Madalena Pinto, Honorina Cidade, Arlene G. Corr¨ºa Structure 13C NMR ̼Æ×Ä£Äâͼ |

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